Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_assertion> ?p ?o ?g. }
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- NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_assertion type Assertion NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_head.
- NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_assertion description "[Here we describe the construction and characterization of DNA libraries for the Langer-Giedion syndrome chromosome region (LGCR, 8q23-24.1), Wilms tumor chromosome region 1 (WT1, 11p13), Prader-Willi syndrome/Angelman syndrome chromosome region (PWCR/ANCR, 15q11.2-12), meningioma chromosome region (MGCR, 22q12-13), and fragile X chromosome region (FRAXA, Xq27.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_provenance.
- NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_assertion evidence source_evidence_literature NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_provenance.
- NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_assertion SIO_000772 2159949 NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_provenance.
- NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_assertion wasDerivedFrom befree-20140225 NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_provenance.
- NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_assertion wasGeneratedBy ECO_0000203 NP758622.RAWhVOsPUKbVzZfHuwozTjO1V5a8wrcgVJ6TNJrJx8dsE130_provenance.